- ManpowerGroup (Rockville, MD)
- Our client, a leader in the pharmaceutical industry, is seeking a Pharma Document Control Associate to join their team. The ideal candidate will have strong ... will align successfully in the organization. **Job Title:** Pharma Document Control Associate **Location:** Rockville, MD **Pay...per respective SOP. + Archive and maintain GLP and GMP documents with an accurate inventory, both on and… more
- Catalent Pharma Solutions (Harmans, MD)
- …are met and leading continuous improvement initiatives. The Document Control function supports both the GMP and development operations. Catalent, ... support Phase I/II/III/commercial operations. + Manages document control processes and systems for GMP activities...document control processes and systems for GMP activities in compliance with internal procedures and policies,… more
- Charles River Laboratories (Rockville, MD)
- …including investigation/deviation management, CAPA tracking, Effectiveness Verification, change control , internal and external audits. This position will facilitate ... and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. **Key Responsibilities and Duties:** *… more
- Charles River Laboratories (Rockville, MD)
- …investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control . This position will facilitate the compiling, trending (as ... industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. Key Responsibilities and Duties: Establishes… more
- Charles River Laboratories (Rockville, MD)
- …investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control . This position will facilitate the compiling, trending (as ... and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. This includes but is not limited… more
- Catalent Pharma Solutions (Harmans, MD)
- …development and implementation of the site Sterility Assurance Program. + Develop, document and manage microbial control strategy for production processes from ... audit observations, aseptic trainings, DE study and sterility assurance/contamination control related GMP documentations. + Drive continuous improvement… more
- Catalent Pharma Solutions (Harmans, MD)
- …recognized tradition of quality and service. Catalent provides process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders ... critical computer systems and laboratory documentation to support the commercial GMP manufacturing of biological drug substance and drug product. Responsibilities… more
- Catalent Pharma Solutions (Harmans, MD)
- …: + Serve as the QA-CSV liaison with the Engineering, Quality Control , IT and Validation organizations to support SaaS enterprise computer systems validation ... and LES modules, Electronic Laboratory Notebook (ELN), OpenText Documentum Electronic Document Management System (EDMS), MODA Software, JDE Edwards etc. + Design… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …related to current Good Manufacturing Practice (cGMP) site audits, quality control and manufacturing (QCM) product documentation reviews, and test design for ... + Conducts thorough review and evaluation of QCM [i.e., quality control and manufacturing] documents and other data received from pharmaceutical, ingredient… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …related to current Good Manufacturing Practice (cGMP) site audits, quality control and manufacturing (QCM) product documentation reviews, and test design. In ... Manufacturing Practice (cGMP) facilities engaged in the manufacturer and/or quality control of dietary supplements and/or pharmaceuticals. * Knowledge of and… more
- Catalent Pharma Solutions (Harmans, MD)
- …Quality Systems to implement equipment, facility, and automation change control , document revisions, and conduct equipment/system/instrumentation failure ... recognized tradition of quality and service. Catalent provides process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders… more
- Charles River Laboratories (Rockville, MD)
- …Records (BPRs) and associated supporting documentation including logbooks, Quality Control (QC) testing reports, environmental monitoring reports, etc. * Support ... to drive completion * Create, review and approve documents in electronic document management systems * Serve as QOps representative for client project teams… more
- Catalent Pharma Solutions (Harmans, MD)
- …of ISO, USP, EU, CFR, cGMP, and GLP in the Microbiology laboratory and GMP Cleanrooms at all times. + Document Environmental Monitoring results utilizing Good ... The **Associate Scientist** will assist with the end-to-end contamination control and sterility assurance practices for Catalent's aseptic production process. This… more
- Charles River Laboratories (Hanover, MD)
- …meet specifications, standards, cost-efficient, with adequate supply for testing. + Document inventory properly and communicate any issues with upper management ... + Manage, log, assign lot numbers (as applicable) and appropriately document all Receipt (incoming) and Shipment (outgoing) of materials, documents, testing… more
- Charles River Laboratories (Bethesda, MD)
- …As the Animal Care Technician II, you will maintain, monitor, and document the health, breeding colony production, technical support, and physical environment within ... all related records, logs, forms, cage cards -Applying quality assurance/quality control standards to ensure Statement of Work expectations are fulfilled **Job… more
- Charles River Laboratories (Bethesda, MD)
- …visits would also be a responsibility of this position. + Identify, document , and/or report environmental or cagewash abnormalities. + Use of computer programs ... by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment.… more
- Charles River Laboratories (Bethesda, MD)
- …multiple animal facilities. As the Technical Trainer you will develop, deliver, document , and report technical skills training programs involving both small and ... by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment.… more